40927-23-9Relevant academic research and scientific papers
SYNTHESIS OF THE PROPIONATES OF (2R,8R)- AND (2S,8R)-8-METHYL-2-DECANOL, THE PHEROMONE OF THE WESTERN CORN ROOTWORM, EMPLOYING CHIRAL COMPOUNDS OF MICROBIAL ORIGIN AS STARTING MATERIALS
Mori, Kenji,Watanabe, Hidenori
, p. 299 - 304 (1984)
The attractants of the western corn rootworm (Diabrotica virgifera virgifera Le Conte), the propionates of (2R,8R)- and (2S,8R)-8-methyl-2-decanol, were synthesized from (R)-(+)-citronellol and the enantiomers of ethyl β-hydroxybutyrate of microbial origin.
SYNTHESIS OF TREE STEREOISOMERIC FORMS OF 2,8- DIMETHYL-1,7-DIOXASPIROUNDECANE, THE MAIN COMPONENT OF THE CEPHALIC SECRETION OF ANDRENA WILKELLA
Mori, Kenji,Tanida, Kaichi
, p. 3221 - 3225 (2007/10/02)
Three stereoisomers of 2,8-dimethyl-1,7-dioxaspiroundecane were synthesized from acetoacetic ester by utilizing its yeast reduction and dianion alkylation.
